Align lysine-specific permease (characterized)
to candidate WP_058931453.1 AU252_RS15260 D-serine/D-alanine/glycine transporter
Query= CharProtDB::CH_003129 (489 letters) >NCBI__GCF_001484605.1:WP_058931453.1 Length = 498 Score = 264 bits (674), Expect = 6e-75 Identities = 165/491 (33%), Positives = 265/491 (53%), Gaps = 31/491 (6%) Query: 1 MVSETKTT--EAPGLRRELKARHLTMIAIGGSIGTGLFVASGATISQAGPGGALLSYMLI 58 M +ET TT P L R+L RH+ +IAIGG+IGTGLF+ SG TIS AGP + YM+I Sbjct: 1 MSTETVTTPGNTPHLERQLSNRHIQLIAIGGAIGTGLFMGSGKTISAAGPS-VIFVYMII 59 Query: 59 GLMVYFLMTSLGELAAYMPVSGSFATYGQNYVEEGFGFALGWNYWYNWAVTIAVDLVAAQ 118 G M++F+M ++GEL SF+ + + + GF GW YW+ W +T D++A Sbjct: 60 GFMLFFVMRAMGELLLSNLHYKSFSDFAADLLGPWAGFFTGWTYWFCWVITGIADVIAIA 119 Query: 119 LVMSWWFPDTPGWIWSALFLGVIFLLNYISVRGFGEAEYWFSLIKVTTVIVFIIVGVLMI 178 +P P WI + ++ +LN +VR FGE E+WF+LIK+ + IIVG+ MI Sbjct: 120 AYSEELWPGVPLWIPGIATVVILLVLNLATVRAFGETEFWFALIKIIAIAALIIVGLFMI 179 Query: 179 IGIFKG-AQPAGWSN-WTIGEAPFAGGFAAMIGVAMIVGFSFQGTELIGIAAGESEDPAK 236 F+ A PA ++N W+ G F F + I F+F G EL+G A E++DP K Sbjct: 180 FSGFQSDAGPATFNNLWSHG-GMFPNEFMGFVAGFQIAVFAFVGIELVGTTAAEAKDPEK 238 Query: 237 NIPRAVRQVFWRILLFYVFAILIISLIIPYTDPSLLRNDVKDISVSPFTLVFQHAGLLSA 296 N+P+A+ + R+LLFYV A++I+ + P+T SPF +F AGL +A Sbjct: 239 NLPKAINSIPIRVLLFYVGALIILMSVTPWTQ--------FQAGHSPFIAMFSLAGLGAA 290 Query: 297 AAVMNAVILTAVLSAGNSGMYASTRMLYTLACDGKAPRIFAKLSRGGVPRNALYATTVIA 356 A ++N V+L++ +S+ NSG+Y+++RM+Y LA +G AP +F++LS VP+NAL+ + ++ Sbjct: 291 ATIVNLVVLSSAMSSANSGIYSTSRMVYGLAQEGDAPTVFSRLSSRKVPQNALFLSCILL 350 Query: 357 GLCFLTSMFGNQTV---YLWLLNTSGMTGFIAWLGIAISHYRF--RRGYVLQGHDINDLP 411 L + M+ + + + + S + W I S+ +F RR ++ H+ + Sbjct: 351 -LSGIVLMYAGKDIGKAFDMVTTVSAVCFVFVWSIILASYLKFRSRRPHL---HESSKYK 406 Query: 412 YRSGFFPLGPIFAFILCLIITLGQNYEAFLKDTIDWGGVAATYIGIPLFLIIWFGYKLIK 471 G + +FAF ++ L + + + T I L + W + + Sbjct: 407 MPGGVPMVWVVFAFFAFVLWALTTQPDTLV-------ALLVTPIWFILLGVAWIILRK-R 458 Query: 472 GTHFVRYSEMK 482 +H RY+E + Sbjct: 459 PSHLARYAEFQ 469 Lambda K H 0.327 0.142 0.451 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 751 Number of extensions: 55 Number of successful extensions: 7 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 489 Length of database: 498 Length adjustment: 34 Effective length of query: 455 Effective length of database: 464 Effective search space: 211120 Effective search space used: 211120 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.1 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory